📌 Key Points
- Natasimham Balayya: ₹16 Cr Child’s Life at Stake!
- Unbelievable: ₹16 Crores for One Life-Saving Shot!
- Rare SMA Type 2: 2-Year-Old Fights for Life!
- Balayya’s Urgent Appeal: Save Keyansh, Contribute Now!
Actor-politician Balakrishna, a familiar face in South Indian cinema, has demonstrated immense humanity by appealing for donations to save a child battling rare SMA Type 2 disease. Learning of the critical condition in his constituency, he promptly offered personal help and now urges the public to contribute, proving himself a real-life hero beyond the silver screen.
Balayya’s Call to Save a Child
Shocking: Balayya’s Call to Save a Child’s Life! A Plea for Donations!! Natasimham Balakrishna has once again demonstrated his profound humanity, proving himself a real-life hero. Upon learning that a child in his constituency was battling a life-threatening condition, he not only immediately responded with an offer of his own help but also issued a heartfelt appeal for public contributions.
The tragedy unfolds in his Hindupur constituency, where 2.5-year-old Keyansh Advik, son of Nataraj and his wife from Lepakshi village, is suffering from an extremely rare and life-threatening disease: Spinal Muscular Atrophy Type 2 (SMA Type 2). Doctors at Bangalore Baptist Hospital confirmed that Keyansh has been battling this condition for the past 21 months. The family recently met Balakrishna during his visit to Hindupur, seeking collective assistance. The life-saving drug required, AVXS-101 (Onasemnogene Abeparvovec), is not manufactured in India, and a single, one-time injection comes with an exorbitant price tag of ₹16 crores—an amount far beyond the family’s means.
Rare SMA Battle: ₹16 Crore Treatment
In response, Balakrishna publicly announced his solidarity with the child and shared a comprehensive appeal on his social media account, Facebook, stating: “Hello everyone… Keyansh Advik (2.5 years old), son of Nataraj and his wife, residents of Lepakshi village in our Hindupur constituency, is suffering from an extremely rare disease called ‘Spinal Muscular Atrophy Type 2’. According to doctors at Bangalore Baptist Hospital, Baby Keyansh Advik has been suffering from this life-threatening rare disease for the past 21 months. The life-saving drug required for this disease, AVXS-101 (Onasemnogene Abeparvovec), is not manufactured in India. The price of this one-time life-saving injection is ₹16 crores. This family met me yesterday during my visit to Hindupur, informed me of their child’s condition, and sought our collective help. Since the family is not in a position to raise such a huge amount of money, I am making my contribution and assuring them that I will also make efforts on the government’s behalf. From a humanitarian perspective, I lovingly appeal to everyone to come forward and take a step towards securing the child’s future with their contribution. Account details: Account- 8265662545, Name – A S Nataraj, IFSC – IDIB000J028, Branch – J P NAGAR.”
Balakrishna’s call highlights the critical need for understanding SMA Type 2 and the urgency of the situation. Let us all respond to this humanitarian appeal from Balakrishna Garu and come forward to contribute our share, helping to secure the child’s future and save his life. Stay tuned for more updates.
Looking Ahead
Balakrishna Garu’s urgent call for this child’s life resonates deeply. Let our collective compassion fuel immediate action against SMA Type 2. We are confident that with unwavering support, a bright, healthy future awaits this child. Humanity, truly, will prevail.
